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Senior Medical Information Associate Italian Language

Role overview

Qualifications

  • Life science / bio medical background – healthcare related degree.
  • Customer service or call centre experience preferred.
  • Strong interpersonal and communication skills.
  • Advanced English skills, both verbal and written.

Responsibilities

  • Provide approved responses to medical enquiries from external customers in Italian and English.
  • Accurately identify, document and report adverse events/side effects, pregnancy and other special situation events.
  • Ensure all medical information enquiries are tracked and documented within the Medical Information database.
  • Assist in departmental regulatory inspection preparedness.

Key facts

Other skills

  • Customer Service
  • Time Management
  • Multitasking
  • Social Skills
  • Communication
  • Problem Solving
  • Detail Oriented
  • Delegation Skills

About the company

PrimeVigilance logo

PrimeVigilance

Contract Research Organizations (CRO)

PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs.From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries.• 900+ highly qualified professionals• Global leader in QPPV services• 24/7 multilingual call center• Choice of leading drug safety databases• Robotic Process Automation (RPA) expertise• Access to regulatory experts and key opinion leadersGLOBAL LIFE CYCLE MANAGEMENT SERVICES• PHARMACOVIGILANCE • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT• AUDIT & INSPECTION• QUALITY MANAGEMENT• REGULATORY SCIENCE

Company details

IndustryContract Research Organizations (CRO)
Company size501 - 1000

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Job description

Company Description

Medicine moves forward here. So will you. 

 

At PrimeVigilance, patient safety is not one part of the job. It is why we exist. 

 

We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on. 

 

That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from. 

 

If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you. 

Job Description

PrimeVigilance is looking for a Medical Information Associate with Italian language to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries. 

Responsibilities:

• To provide approved responses to medical enquiries from external customers (healthcare professionals, patients, pharmaceutical clients) including call handling in Italian and English.

• To accurately identify, document and report adverse events/side effects, pregnancy and other special situation events, and product quality complaints within required timeframes 

• To ensure that all medical information enquiries are tracked and fully documented within the Medical Information database accurately and completely 

• To participate in the out-of-hours provision of medical information for clients who have contracted a 24/7 enquiry handling service 

 • Providing management with regular updates regarding project status and metrics concerning enquiries 

• Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits  

Qualifications

  • Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, pharmacy, nursing) 

  • Customer service or call centre experience preferred 

  • Comfortable receiving enquires by phone 

  • Ability to perform out-of-hours service if required 

  • Time and issue management, delegation, organization and multitasking skills with good attention to detail 

  • Strong interpersonal and communication skills 

  • Advanced English skills, both verbal and written

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

 

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

 

  • Quality: we hold ourselves to the standard patients deserve. 

  • Integrity and trust: we do the right thing, especially when it is hard. 

  • Drive and passion: we care about the outcome, because someone is waiting on it. 

  • Agility and responsiveness: we move quickly, because patients cannot wait. 

  • Belonging: everyone is welcome, and every voice counts. 

  • Collaborative partnerships: we go further by going together. 

 

We look forward to welcoming your application. 

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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